Variant #0000328890 (NC_000022.10:g.20104513_20104531del, NM_001190326.1:c.*6882_*6900del (DGCR8))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.20104513_20104531del
DNA change (hg38) g.20116990_20117008del
Published as TRMT2A(NM_001257994.1):c.-82_-64del (p.(=))
ISCN -
DB-ID RANBP1_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DGCR8 NM_001190326.1 ?/. - c.*6882_*6900del r.(=) p.(=)
RANBP1 NM_002882.2 ?/. - c.-660_-642del r.(?) p.(=)
DGCR8 NM_022720.6 ?/. - c.*6882_*6900del r.(=) p.(=)
TRMT2A NM_022727.5 ?/. - c.-82_-64del r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.